Skip Navigation

This Article
Right arrow Print PDF (2667K)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Commercial Re-use Guidelines
for Open Access NAR Content
Google Scholar
Right arrow Articles by Böhnlein, E.
Right arrow Articles by Gruss, P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Böhnlein, E.
Right arrow Articles by Gruss, P.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Nucleic Acids Research, 1985, Vol. 13, No. 13 4789-4809
© 1985


Articles

Functional analysis of the regulatory region of polyoma mutant F9-1 DNA

Ernst Böhnlein, Kamal Chowdhury and Peter Gruss

Zentrum für Molekulare Biologie der Universität Heidelberg Im Neuenheimer Feld 364, D-6900 Heidelberg, FRG

Received March 27, 1985. Revised June 14, 1985. Accepted June 14, 1985.

Functional analysis of the transcriptional control region of the polyoma (Py) mutant F9-1 reveals that the mutation is located in a region of Py DNA required for at least two functions. First, an enhancer element which includes the F9-1 mutation was characterized by deletion analysis. This element, described previously as enhancer B (1,2) is essential for viral early gene expression in F9 stem cells whereas enhancer A is unnecessary for transcriptional activity in embryonal carcinoma (EC) cells. Second, a CCACCC motif, present twice in the 3' part of enhancer B is also required in cis for the response to a heterologous enhancer. This suggests that a promoter element is present in this region of the polyoma genome which overlaps Py enhancer B. We also demonstrate the enhancement of the polyoma early promoter activity in F9 stem cells by M8V sequences. The significance of these observations is discussed.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
ScienceHome page
J. Moyer, M. Lee-Tischler, H. Kwon, J. Schrick, E. Avner, W. Sweeney, V. Godfrey, N. Cacheiro, J. Wilkinson, and R. Woychik
Candidate gene associated with a mutation causing recessive polycystic kidney disease in mice
Science, May 27, 1994; 264(5163): 1329 - 1333.
[Abstract] [PDF]



Disclaimer:
Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.